ACAD9 基因新发变异致线粒体复合物 I 缺乏症20 型1 例报告并文献复习

崔清洋，曹银利，唐成和，等

Mitochondrial complex I deficiency nuclear type 20 caused by a novel variation of ACAD9 gene: a case report and literature review

CUI Qingyang, CAO Yinli, TANG Chenghe, et al

临床儿科杂志 . 2021, (7): 538 . DOI: 10.3969/j.issn.1000-3606.2021.07.014